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Visualizing endogenous Rho activity with an improved localization-based, genetically encoded biosensor

Rho GTPases are regulatory proteins, which orchestrate cell features such as morphology, polarity and movement. Therefore, probing Rho GTPase activity is key to understanding processes such as development and cell migration. Localization-based reporters for active Rho GTPases are attractive probes t...

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Autores principales: Mahlandt, Eike K., Arts, Janine J. G., van der Meer, Werner J., van der Linden, Franka H., Tol, Simon, van Buul, Jaap D., Gadella, Theodorus W. J., Goedhart, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445605/
https://www.ncbi.nlm.nih.gov/pubmed/34357388
http://dx.doi.org/10.1242/jcs.258823
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author Mahlandt, Eike K.
Arts, Janine J. G.
van der Meer, Werner J.
van der Linden, Franka H.
Tol, Simon
van Buul, Jaap D.
Gadella, Theodorus W. J.
Goedhart, Joachim
author_facet Mahlandt, Eike K.
Arts, Janine J. G.
van der Meer, Werner J.
van der Linden, Franka H.
Tol, Simon
van Buul, Jaap D.
Gadella, Theodorus W. J.
Goedhart, Joachim
author_sort Mahlandt, Eike K.
collection PubMed
description Rho GTPases are regulatory proteins, which orchestrate cell features such as morphology, polarity and movement. Therefore, probing Rho GTPase activity is key to understanding processes such as development and cell migration. Localization-based reporters for active Rho GTPases are attractive probes to study Rho GTPase-mediated processes in real time with subcellular resolution in living cells and tissue. Until now, relocation Rho biosensors (sensors that relocalize to the native location of active Rho GTPase) seem to have been only useful in certain organisms and have not been characterized well. In this paper, we systematically examined the contribution of the fluorescent protein and Rho-binding peptides on the performance of localization-based sensors. To test the performance, we compared relocation efficiency and specificity in cell-based assays. We identified several improved localization-based, genetically encoded fluorescent biosensors for detecting endogenous Rho activity. This enables a broader application of Rho relocation biosensors, which was demonstrated by using the improved biosensor to visualize Rho activity during several cellular processes, such as cell division, migration and G protein-coupled receptor signaling. Owing to the improved avidity of the new biosensors for Rho activity, cellular processes regulated by Rho can be better understood. This article has an associated First Person interview with the first author of the paper.
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spelling pubmed-84456052021-09-21 Visualizing endogenous Rho activity with an improved localization-based, genetically encoded biosensor Mahlandt, Eike K. Arts, Janine J. G. van der Meer, Werner J. van der Linden, Franka H. Tol, Simon van Buul, Jaap D. Gadella, Theodorus W. J. Goedhart, Joachim J Cell Sci Tools and Resources Rho GTPases are regulatory proteins, which orchestrate cell features such as morphology, polarity and movement. Therefore, probing Rho GTPase activity is key to understanding processes such as development and cell migration. Localization-based reporters for active Rho GTPases are attractive probes to study Rho GTPase-mediated processes in real time with subcellular resolution in living cells and tissue. Until now, relocation Rho biosensors (sensors that relocalize to the native location of active Rho GTPase) seem to have been only useful in certain organisms and have not been characterized well. In this paper, we systematically examined the contribution of the fluorescent protein and Rho-binding peptides on the performance of localization-based sensors. To test the performance, we compared relocation efficiency and specificity in cell-based assays. We identified several improved localization-based, genetically encoded fluorescent biosensors for detecting endogenous Rho activity. This enables a broader application of Rho relocation biosensors, which was demonstrated by using the improved biosensor to visualize Rho activity during several cellular processes, such as cell division, migration and G protein-coupled receptor signaling. Owing to the improved avidity of the new biosensors for Rho activity, cellular processes regulated by Rho can be better understood. This article has an associated First Person interview with the first author of the paper. The Company of Biologists Ltd 2021-09-08 /pmc/articles/PMC8445605/ /pubmed/34357388 http://dx.doi.org/10.1242/jcs.258823 Text en © 2021. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Tools and Resources
Mahlandt, Eike K.
Arts, Janine J. G.
van der Meer, Werner J.
van der Linden, Franka H.
Tol, Simon
van Buul, Jaap D.
Gadella, Theodorus W. J.
Goedhart, Joachim
Visualizing endogenous Rho activity with an improved localization-based, genetically encoded biosensor
title Visualizing endogenous Rho activity with an improved localization-based, genetically encoded biosensor
title_full Visualizing endogenous Rho activity with an improved localization-based, genetically encoded biosensor
title_fullStr Visualizing endogenous Rho activity with an improved localization-based, genetically encoded biosensor
title_full_unstemmed Visualizing endogenous Rho activity with an improved localization-based, genetically encoded biosensor
title_short Visualizing endogenous Rho activity with an improved localization-based, genetically encoded biosensor
title_sort visualizing endogenous rho activity with an improved localization-based, genetically encoded biosensor
topic Tools and Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8445605/
https://www.ncbi.nlm.nih.gov/pubmed/34357388
http://dx.doi.org/10.1242/jcs.258823
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